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Six months post cure, splenocytes from WEHI-164 and K7M2-cured mice were assayed, against WEHI-164 and K7M2 tumor cell lines for in vitro cytotoxicity by using a Cr release standard cytotoxic assay (see Materials and Methods).
This can be explained by a post cure process of adhesive material, activated by UV irradiation.
According previous work [25], ultraviolet exposure influences on the adhesive properties and the action of post cure process promotes an increase in mechanical strength.
In a limited amount of testing, it was observed that temperature shifts caused more rapid stress relaxation rates and that post cure of the composite is essential to achieve a stable thermal response.
For cell-mediated cytotoxicity assay, we used splenocytes from tumor-cured mice 12 days after a tumor booster with the same tumor cells, 6 months post cure, as previously reported 28.
Following the photomasked exposure and subsequent ethanol wash, all of the micropatterned samples were treated with a 10 min post cure to maximize the double bond conversion under the given reaction conditions.
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Oliveira et al. [ 32] showed that FC had a better performance compared to IFA in the monitoring of specific post therapeutic cure of CL.
It influences on the post curing process of the adhesive used increasing shear properties.
Samples were post cured in a UV oven for 30 min.
Thermal stability was investigated by post curing samples at 121 °C and assessing healing performance.
Elevated temperature post curing is one of the most critical step in the processing of polymer composites.
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